Graduate School of Natural Science and Technology, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan.
Chem Commun (Camb). 2019 Sep 19;55(76):11386-11389. doi: 10.1039/c9cc06025a.
A pair of novel optically active triptycene-based molecules ((R,R)-1 and (S,S)-1) containing two hexabenzocoronene moieties were synthesized and their optical and chiroptical properties were investigated. Optically active 1 emitted preferred-handed circularly polarized light upon UV irradiation, with the luminescence dissymmetry factors found to be approximately 1.0 × 10-3. Based on a comparative study using the analogous triptycene derivative with two hexaphenylbenzene units (2), which was the key precursor of 1, the ladder-type rigid structure with an asymmetrically bent geometry was important for optically active 1 to exhibit circularly polarized luminescence (CPL). We also showed that rac-1 undergoes conglomerate crystallization, which allowed CPL to be produced by a random selection of crystals prepared from rac-1.
一对新型的含有两个六苯并蒄部分的手性三并苯基分子((R,R)-1 和 (S,S)-1)被合成出来,并研究了它们的光学和手性光学性质。手性 1 在紫外光照射下发射出优选手性的圆偏振光,其发光不对称因子约为 1.0×10-3。通过使用具有两个六苯基苯部分的类似三并苯衍生物 (2) 进行比较研究,2 是 1 的关键前体,梯型刚性结构和不对称弯曲几何形状对于手性 1 表现出圆偏振发光 (CPL) 很重要。我们还表明,rac-1 经历了聚集体结晶,这使得 CPL 可以通过从 rac-1 制备的晶体的随机选择来产生。